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Phenotypes Associated with This Genotype
Genotype
MGI:5438707
Allelic
Composition
Kdm6atm1a(EUCOMM)Jhha/Kdm6atm1b(EUCOMM)Jhha
Tg(Pgk1-cre)1Lni/0
Genetic
Background
involves: 129 * BALB/c * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kdm6atm1a(EUCOMM)Jhha mutation (0 available); any Kdm6a mutation (40 available)
Kdm6atm1b(EUCOMM)Jhha mutation (0 available); any Kdm6a mutation (40 available)
Tg(Pgk1-cre)1Lni mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• severe closure defect at E11.5

embryo
• severe closure defect at E11.5


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory